Hs02722299_cn

• Gene Symbol: AVEN
• Assay Reference Genome Location: Chr.15:33866147 on build GRCh38
• Cytoband: 15q14

Target Gene Details

• Entrez Gene ID: 57099
• Gene Name: apoptosis and caspase activation inhibitor
• Gene Aliases: PDCD12
• Location: Chr.15:33858602-34074877 on Build GRCh38
• Assay Gene Location:

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
AVEN

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv471235	Chr.15:33743328 - 34129750 on Build GRCh38	Gain	PGBD4 CHRM5 EMC7 RYR3 AVEN
nsv1052620	Chr.15:32612402 - 34538731 on Build GRCh38	Gain	FMN1 MIR1233-1 LPCAT4 SLC12A6 SCG5 LOC100131315 LOC101928042 EMC7 RYR3 GREM1 GOLGA8B TMCO5B MIR1233-2 EMC4 KATNBL1 PGBD4 CHRM5 ARHGAP11A NOP10 NUTM1 AVEN LOC105370757 LOC101928134 GOLGA8A
esv33337	Chr.15:31689863 - 34575097 on Build GRCh38	Gain+Loss	LPCAT4 LOC100131315 LOC101928042 EMC7 RYR3 GOLGA8B GOLGA8N WHAMMP1 GOLGA8K LOC100996255 ULK4P1 AVEN LOC101928134 GOLGA8A FMN1 MIR1233-1 SLC12A6 SCG5 CHRNA7 LOC101060588 GOLGA8O GREM1 TMCO5B MIR1233-2 EMC4 KATNBL1 PGBD4 CHRM5 ARHGAP11A NOP10 NUTM1 LOC100653133 LOC105370757 LOC105370940
nsv568921	Chr.15:33754434 - 33955421 on Build GRCh38	Gain	RYR3 AVEN
esv3569431	Chr.15:33564570 - 35080307 on Build GRCh38	Gain	LOC101928174 MIR1233-1 LPCAT4 SLC12A6 EMC7 RYR3 GOLGA8B MIR1233-2 EMC4 AQR KATNBL1 PGBD4 CHRM5 GJD2 NOP10 ZNF770 NUTM1 AVEN GOLGA8A ACTC1
nsv1044844	Chr.15:33773323 - 34004628 on Build GRCh38	Loss	CHRM5 RYR3 AVEN
nsv568920	Chr.15:33742220 - 34134417 on Build GRCh38	Gain	PGBD4 CHRM5 EMC7 RYR3 AVEN
dgv4456n54	Chr.15:32604149 - 34557061 on Build GRCh38	Gain	LPCAT4 LOC100131315 LOC101928042 EMC7 RYR3 GOLGA8B GOLGA8N AVEN LOC101928134 GOLGA8A FMN1 MIR1233-1 SLC12A6 SCG5 GREM1 TMCO5B MIR1233-2 EMC4 KATNBL1 PGBD4 CHRM5 ARHGAP11A NOP10 NUTM1 LOC105370757

More Information

Additional Information:

For this assay, SNP(s) [rs116671589] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Non-exonic, DGV Variation